510(k) K760757 ยท DXY Implantable Pacemaker Pulse-Generator
MODEL 100 CARDIAC PACEMAKER
| Applicant | Pacesetter Systems, Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 11, 1976 |
| Received | Oct 1, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K760757
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.